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NOT YET RECRUITING
NCT07803536
NA

Effect of Late Ripcord Removal From Glaucoma Drainage Device

Sponsor: Duke University

View on ClinicalTrials.gov

Summary

This is a research study to find out if removing the ripcord from a glaucoma drainage device more than 3 months after it has been placed has any effect on intraocular pressure. Participation in research studies is voluntary. The ripcord will be removed at a routine glaucoma care visit and intraocular pressure will be measured before removal, 30 minutes following, and at 1 week, 6 weeks and 3-month intervals during regular clinic visits.

Official title: Prospective, Single-arm Interventional Study to Determine Effect of Late Ripcord Removal From Glaucoma Drainage Device

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2026-09

Completion Date

2028-12

Last Updated

2026-09-03

Healthy Volunteers

No

Interventions

PROCEDURE

Ripcord removal

Patients who have had a ripcord in place for greater than 3 months postoperatively will undergo ripcord removal in the office.

Locations (1)

Duke University Eye Center

Durham, North Carolina, United States